{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Turku",
      "state": "N/A",
      "country": "Finland",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79198",
      "recalling_firm": "PerkinElmer Life and Analytical Sciences, Wallac, OY",
      "address_1": "Mustionkatu 6",
      "address_2": "P.O. Box 10",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to CT and TX.",
      "recall_number": "Z-1220-2018",
      "product_description": "AutoDELFIA Neonatal immunoreactive trypsin(ogen) (IRT) kit, intended for the quantitative determination of human immunoreactive trypsin(ogen) (IRT) in blood specimens. (UDI: (01)06438147298716(17)190430(10)656479); Product Number: B005-212",
      "product_quantity": "240",
      "reason_for_recall": "The Quality Control Certificate for certain AutoDELFIA Neonatal IRT Kits is missing information required to assess the acceptability of measured control values which may result in a delay in reporting IRT results.",
      "recall_initiation_date": "20170925",
      "center_classification_date": "20180831",
      "termination_date": "20180906",
      "report_date": "20180912",
      "code_info": "Lot Number: 656479, Batch Number: 1065647901, Expiration date: 2019-4-30"
    }
  ]
}